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Uzpruvo® for your
Dermatology / Rheumatology patients

Introducing Uzpruvo®:
The New Ustekinumab Biosimilar

Uzpruvo® is currently not approved for the ulcerative colitis indication (since the originator still has exclusivity for this indication)

Mode of Action
Plaque Psoriasis
and Paediatric
Plaque Psoriasis
Psoriatic
Arthritis

UNIQUE mode of action of ustekinumab:
IL12/IL23-receptor binding inhibition

Ustekinumab is a fully human IgG1κ monoclonal antibody that binds with specificity to the shared p40 protein subunit of pro-inflammatory cytokines IL-12 and IL-23 to prevent them from binding to their receptors, expressed on the surface of immune cells, therefore inhibiting inflammatory processes early1

Dosing

UZPRUVO® IN DERMATOLOGY & RHEUMATOLOGY
POSOLOGY OPTIONS1

Choose between two dose strengths to suit individual treatment needs

Maintenance:
SC Injection*
sc injection
Presentation:
Pre-filled Syringe
sc injection

SC, subcutaneous

Dosing1

BW, body weight; PFS, pre-filled syringe; Q12W, every 12 weeks; SC, subcutaneous
1. Uzpruvo® SmPC (Feb. 2024).

Comparatively Fewer Treatments:
Dermatology & Rheumatology Treatment Regimes1-3

Example of total doses in the first year of treatment (52 weeks) for adult patients with Crohn's disease

Q2W, every 2 weeks; Q4W, every 4 weeks; Q12W, every 12 weeks; SC, subcutaneous; W, week(s)
*Uzpruvo® weight-based dosage regime: BW ≤100 kg: 45 mg, BW 100 kg: 90 mg;
**Numbers based on the use of a 300 mg dosage. Secukinumab weight-based dosage frequency is Q4W for patient with BW 90 kg and Q2W with BW ≥90 kg2
1. Uzpruvo® SmPC (Feb. 2024); 2. Cosentyx® SmPC (Aug. 2023); 3. Taltz® SmPC (Feb. 2023).

Phase III Trial

Adapted from Feldman SR et al. 20231
BL, baseline; BSA, body surface area; DLQI, Dermatology life quality index; EoS, end of study; PASI, Psoriasis Area and Severity Index; Q12W, every 12 weeks; SC, subcutaneous; sPGA, statistic physician's global assessment
*Stelara®; **≤100 kg body weight: 45 mg, >100 kg body weight: 90 mg
1. Feldman SR et al. Expert Opin Biol Ther. 2023;23(3):253-60. DOI: 10.1080/14712598.2023.2235263.

Safety

Adapted from Feldman SR et al. 20231
AE, adverse event; RP, reference product; TEAE, treatment-emergent adverse event
*Stelara® 1. Feldman SR et al. Expert Opin Biol Ther. 2023;23(3):253-60. DOI: 10.1080/14712598.2023.2235263.

Date prepared: June 2024. 2024/ADV/UZP/155H